Variant report

Variant	rs2966479
Chromosome Location	chr7:112290310-112290311
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10224255	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1234383	0.87[ASN][1000 genomes]
rs1613412	0.88[ASN][1000 genomes]
rs1796502	0.88[CHB][hapmap];0.81[ASN][1000 genomes]
rs1922899	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1922902	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2188550	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2188551	0.82[ASN][1000 genomes]
rs2905285	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2905288	0.81[ASN][1000 genomes]
rs2905291	0.81[ASN][1000 genomes]
rs2952682	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2952683	0.89[ASN][1000 genomes]
rs2966480	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2966482	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2966483	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs977478	0.92[ASN][1000 genomes]
rs977479	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs977480	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531436	chr7:111856171-112585407	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	105 gene(s)	inside rSNPs	diseases
2	nsv889055	chr7:112174089-112353440	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:112289000-112294800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:112289000-112295000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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